Annotation Detail
Information
- Associated Genes
- POU1F1
- Associated Variants
-
POU1F1 p.Arg297Trp (p.R297W)
(
ENST00000350375.7,
ENST00000560656.1,
ENST00000344265.8 )
POU1F1 p.Arg297Trp (p.R297W) ( ENST00000344265.8, ENST00000350375.7, ENST00000560656.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000306.4(POU1F1):c.811C>T (p.Arg271Trp) AND not provided
- ClinVar Allele ID
- 28642
- ClinVar RefSeq Alternation Syntax
- NM_000306.4:c.811C>T
- ClinVar RefSeq Alternation Syntax
- NM_001122757.3:c.889C>T
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2016-11-16
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000591288
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs